Nidek EC-5000 Excimer Laser System

Excimer Laser System

FDA Premarket Approval P970053 S017

This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.

Pre-market Approval Supplement Details

Approval for the change of laser head of the excimer laser, software upgrade to accommodate the laser head change, change of the pc and change to the power transformer.

DeviceNidek EC-5000 Excimer Laser System
Classification NameExcimer Laser System
Generic NameExcimer Laser System
ApplicantNIDEK CO., LTD.
Date Received2017-07-17
Decision Date2018-01-12
PMAP970053
SupplementS017
Product CodeLZS
Advisory CommitteeOphthalmic
Supplement TypeNormal 180 Day Track
Supplement ReasonChange Design/components/specifications/material
Expedited ReviewNo
Combination Product No
Applicant Address NIDEK CO., LTD. 34-14 Maehama, Hiroishi-cho gamagori, Aichi 443-0-0038

Supplemental Filings

Supplement NumberDateSupplement Type
P970053Original Filing
S017 2017-07-17 Normal 180 Day Track
S016 2017-03-13 Real-time Process
S015 2014-10-03 Normal 180 Day Track
S014 2014-08-18 Real-time Process
S013 2014-02-11 Normal 180 Day Track
S012 2012-09-25 Normal 180 Day Track
S011 2007-03-30 Panel Track
S010 2006-08-08 Normal 180 Day Track
S009 2005-11-23 Panel Track
S008 2004-04-19 Real-time Process
S007 2002-05-23 Normal 180 Day Track
S006 2001-03-15 Normal 180 Day Track
S005 2001-01-30 Normal 180 Day Track
S004
S003 2000-04-28 Normal 180 Day Track
S002 1999-04-19 Panel Track
S001 1999-02-16 Panel Track

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